Evidence map›Paper›PMID 12368215›Full record

ArticleThe American journal of pathology2002

Matrix metalloproteinase-9-dependent exposure of a cryptic migratory control site in collagen is required before retinal angiogenesis.

Masanori Hangai, Norihiko Kitaya, Jingsong Xu, Candy K Chan, Jenny J Kim, Zena Werb, Stephen J Ryan, Peter C Brooks

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
13.3field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

42 citing papers in PubMed, 130 citations in OpenAlex.

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  16. Extracellular matrix and fibroblast communication following myocardial infarction.Journal of cardiovascular translational research · 2012
    Review
  17. Article
  18. Article
  19. Article
  20. Matrix metalloproteinases and peripheral arterial disease.Internal and emergency medicine · 2010
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 2 countries.

Masanori HangaiDepartment of Ophthalmology, Kobe City General Hospital, Kobe, Japan.
Norihiko Kitaya
Jingsong Xu
Candy K Chan
Jenny J Kim
Zena Werb
Stephen J Ryan
Peter C Brooks
Doheny Eye Institute · USNew York University · USUniversity of California, San Francisco · USUniversity of Southern California · US

Funding

VISION RESEARCHP30EY003040 · NEI · DOHENY EYE INSTITUTE · PI SUN, DEMING · 1985 to 2013
$7.0M
EXPERIMENTAL APPROACH TO MACULOPATHYR01EY001545 · NEI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI HINTON, DAVID R. · 1985 to 2016
$6.0M
CRYPTIC DOMAINS OF COLLAGEN IV IN TUMOR GROWTHR01CA091645 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI BROOKS, PETER C. · 2000 to 2011
$3.3M
PROTEOLYZED COLLAGEN IN ANGIOGENESIS AND APOPTOSISR29CA074132 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI BROOKS, PETER C. · 1997 to 2001
$230k
NCI NIH HHS CA74132NCI NIH HHS CA91645NCI NIH HHS R01 CA091645NEI NIH HHS EY01545NEI NIH HHS EY03040NEI NIH HHS P30 EY003040NEI NIH HHS R01 EY001545
6 · The paper itself

Abstract

Retinal neovascularization is a leading cause of human blindness. However, little is known concerning the molecular mechanisms controlling retinal neovascularization in vivo. Here we provide evidence that exposure of a collagen type IV cryptic epitope detected by monoclonal antibody (mAb) HUIV26, delineates sites of vascular bud formation and represents one of the earliest structural remodeling events required before vessel out-growth. Exposure of these cryptic sites was inhibited in matrix metalloproteinase (MMP)-9-deficient but not MMP-2-deficient mice implicating MMP-9 in their exposure. Retinal endothelial cell interactions with the HUIV26 epitopes induced endothelial cell migration, which was blocked by mAb HUIV26. Importantly, subcutaneous administration of mAb HUIV26 potently inhibited retinal angiogenesis in vivo. Taken together, these findings suggest a novel mechanism in which MMP-9 facilitates exposure of HUIV26 cryptic sites, thereby promoting retinal endothelial cell migration and neovascularization in vivo.

Indexed as

AnimalsBlindnessCattleCell MovementCells, CulturedCollagenEndothelium, VascularGelatinHumansIschemiaMatrix Metalloproteinase 9MiceMice, KnockoutNeovascularization, PathologicProtein IsoformsRetinal VesselsCollagenGelatinMatrix Metalloproteinase 9Protein Isoforms

Identifiers

PMID12368215
PMCPMC1867273
OpenAlexW2030334714

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.